50640
Glycolic acid nitrile solution
~70% in H2O
Synonym(s):
Formaldehyde cyanohydrin, Hydroxyacetonitrile
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10 ML
€93.40
50 ML
€357.00
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10 ML
€93.40
50 ML
€357.00
About This Item
Linear Formula:
HOCH2CN
CAS Number:
Molecular Weight:
57.05
Beilstein:
605328
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
contains
~0.5% phosphoric acid as stabilizer
Quality Level
concentration
~70% in H2O
refractive index
n20/D 1.389
density
1.076 g/mL at 20 °C
functional group
hydroxyl
nitrile
SMILES string
OCC#N
InChI
1S/C2H3NO/c3-1-2-4/h4H,2H2
InChI key
LTYRAPJYLUPLCI-UHFFFAOYSA-N
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General description
The product is a 70% solution of glycolic acid nitrile in water. Glycolic acid nitrile, also known as hydroxyacetonitrile is the simplest cyanohydrin.[1] The microwave spectra of hydroxyacetonitrile have been recorded in gas-phase and its rotational constants have been calculated.[2] Ice containing formaldehyde and hydrogen cyanide react under astrophysical-like conditions to form hydroxyacetonitrile.[3][4]
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 2 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral
Storage Class Code
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
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Microwave and Quantum-Chemical Study of Conformational Properties and Intramolecular Hydrogen Bonding of 2-Hydroxy-3-Butynenitrile (HC=CCH(OH)C=N).
M?llendal H, et al.
The Journal of Physical Chemistry A, 119(4), 634-640 (2015)
Formation of hydroxyacetonitrile (HOCH2CN) and polyoxymethylene (POM)-derivatives in comets from formaldehyde (CH2O) and hydrogen cyanide (HCN) activated by water.
Danger G, et al.
Physical Chemistry Chemical Physics, 16(8), 3360-3370 (2014)
Hydroxyacetonitrile (HOCH2CN) formation in astrophysical conditions. competition with the aminomethanol, a glycine precursor.
Danger G, et al.
The Astrophysical Journal, 756(1), 11-11 (2012)
Rotational isomerism and barriers to internal rotation in hydroxyacetonitrile from microwave spectroscopy.
Cazzoli G, et al.
J. Chem. Soc., Faraday II, 69, 569-578 (1973)
Acceleration of HCN oligomerization by formaldehyde and related compounds: implications for prebiotic syntheses.
A W Schwartz et al.
Journal of molecular evolution, 18(5), 351-353 (1982-01-01)
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